Category
page 1Organic redox reactions
hydrogenation
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Steps in the hydrogenation of a C=C double bond at a catalyst surface, for example Ni or Pt :
(1) The reactants are Adsorption|adsorbed on the catalyst surface and H2 dissociates.
(2) An H atom bonds to one C atom. The other C atom is still attached to the surface.
(3) A second C atom bonds to an H atom. The molecule leaves the surface.
Cannizzaro reaction
organic chemical reaction
Fischer-Tropsch process
chemical reactions that convert carbon monoxide and hydrogen into liquid hydrocarbons

hydroxylation
In chemistry, hydroxylation refers to the installation of a hydroxyl group () into an organic compound. Hydroxylations generate alcohols and phenols, which are very common functional groups. Hydroxylation confers some degree of water-solubility. Hydroxylation of a hydrocarbon is an oxidation, thus a step in degradation.
Clemmensen reduction
organic redox reaction
Sabatier reaction
methanation process of carbon dioxide with hydrogen
haloform reaction
chemical reaction
lipid peroxidation
reaction(s) leading to production of (phospho)lipid peroxides
Birch reduction
organic reaction used to convert arenes to cyclohexadienes
Rosenmund reduction
chemical reaction
Kolbe electrolysis
organic reaction
Sharpless epoxidation
chemical reaction

autoxidation
Autoxidation (sometimes auto-oxidation) refers to oxidations brought about by reactions with oxygen at normal temperatures, without the intervention of flame or electric spark. The term is usually used to describe the gradual degradation of organic compounds in air at ambient temperatures. Many common phenomena can be attributed to autoxidation, such as food going rancid, the 'drying' of varnishes and paints, and the perishing of rubber. It is also an important concept in both industrial chemistry and biology. Autoxidation is therefore a fairly broad term and can encompass examples of photooxy
Leuckart reaction
Chemical reaction
Bouveault–Blanc reduction
Type of chemical reaction
Wacker process
chemical reaction
Sharpless asymmetric dihydroxylation
chemical reaction
Acyloin condensation
Condensation reaction
Bosch reaction
forms elemental carbon from CO2 and hydrogen using a metallic catalyst
reductive amination
chemical reaction
Staudinger reaction
chemical reaction
Hydrogenolysis
Hydrogenolysis is a chemical reaction whereby a carbon–carbon or carbon–heteroatom single bond is cleaved or undergoes lysis (breakdown) by hydrogen. The heteroatom may vary, but it usually is oxygen, nitrogen, or sulfur. A related reaction is hydrogenation, where hydrogen is added to the molecule, without cleaving bonds. Usually hydrogenolysis is conducted catalytically using hydrogen gas.
Eschweiler–Clarke reaction
named for the German chemist Wilhelm Eschweiler
Andrussow process
chemical process

aromatization
Aromatization is a chemical reaction in which an aromatic system is formed from a single nonaromatic precursor. Typically aromatization is achieved by dehydrogenation of existing cyclic compounds, illustrated by the conversion of cyclohexane into benzene. Aromatization includes the formation of heterocyclic systems.
center|422px|thumb|The conversion of methylcyclohexane to [[toluene is a classic aromatization reaction. This platinum (Pt)-catalyzed process is practiced on scale in the production of gasoline from petroleum.]]
Étard reaction
Oxidisation reaction
alcohol oxidation
chemical reaction
Emde degradation
chemical reaction
organic redox reaction
redox reaction that takes place with organic compounds
Kiliani–Fischer synthesis
method for synthesizing longer monosaccharides
Zinin reaction
conversion of nitro aromates like nitrobenzene to amines by reduction with sodium sulfides

Bechamp reduction
chemical configuration

Wohl–Aue reaction
chemical reaction
Kornblum oxidation
chemical reaction

Barton–McCombie deoxygenation
Organic reaction
Luche reduction
primary alcohol
Stephen aldehyde synthesis
chemical reaction
Sharpless oxyamination
Chemical reaction
Corey–Winter olefin synthesis
series of chemical reactions for converting 1,2-diols into olefins
Algar–Flynn–Oyamada reaction
chemical reaction producing flavonol
Angeli–Rimini reaction
chemical reaction
Shapiro reaction
organic reaction
omega oxidation
Metabolic process in some animals

Bergmann degradation
chemical reaction
Wolffenstein–Böters reaction
organic reaction converting benzene to picric acid
Prévost reaction
chemical reaction
transfer hydrogenation
chemical process
Adkins–Peterson reaction
Wharton reaction
chemical reaction

Akabori amino-acid reaction
type of amino acid reaction
Benkeser reaction
Organic reduction reaction
Grundmann aldehyde synthesis
Type of chemical reaction
McFadyen–Stevens reaction
chemical reaction
DL-methionine (RS)-S-oxide
group of stereoisomers
Whiting reaction
chemical reaction
Glycol cleavage
type of organic chemistry oxidation
Mozingo reduction
chemical reaction capable of fully reducing a ketone or aldehyde to the corresponding alkane
deoxygenation
Deoxygenation is a chemical reaction involving the removal of oxygen atoms from a molecule. The term also refers to the removal of molecular oxygen (O2) from gases and solvents, a step in air-free technique and gas purifiers. As applied to organic compounds, deoxygenation is a component of fuels production as well a type of reaction employed in organic synthesis, e.g. of pharmaceuticals.
Reduction of nitro compounds
chemical reaction
amide reduction
organic reaction where amide is converted to Amine or Aldehyde